What is another word for crouzon syndrome?
Pronunciation: [kɹˈuːzɒn sˈɪndɹə͡ʊm] (IPA) 
Crouzon Syndrome, also known as dysostosis craniofacialis, is a rare genetic disorder that affects the development of the skull, causing it to fuse early and leading to facial abnormalities such as underdeveloped upper jaw, bulging eyes, and a flattened forehead. While the condition is commonly referred to as Crouzon Syndrome, it is also known as craniofacial dysostosis or craniofacial dysplasia. Other synonyms for Crouzon Syndrome include craniofacial anomalies, maxillary hypoplasia, and syndromic craniosynostosis. While there is currently no cure for the rare condition, early diagnosis and treatment can help manage symptoms and improve quality of life for those affected by Crouzon Syndrome.
